U.S. patent application number 16/855888 was filed with the patent office on 2020-10-22 for thermoplastic elastomer composition.
The applicant listed for this patent is Polymax TPE LLC. Invention is credited to Qianqian Li, Yun Martin Lu, Xin Zhang, Xiaofeng Zheng.
Application Number | 20200332096 16/855888 |
Document ID | / |
Family ID | 1000004793799 |
Filed Date | 2020-10-22 |
United States Patent
Application |
20200332096 |
Kind Code |
A1 |
Lu; Yun Martin ; et
al. |
October 22, 2020 |
THERMOPLASTIC ELASTOMER COMPOSITION
Abstract
A thermoplastic elastomer composition and method of making the
thermoplastic elastomer are disclosed. The thermoplastic elastomer
may comprise a polymer blend. The polymer bland may comprise a
non-crosslinked elastomer, oil, polyethylene, and antioxidant. The
oil may be from about 15 wt. % to about 50 wt, % oil. The
polyethylene may be from about 3 wt. % to about 30 wt. %. The
antioxidant may be from about 0 to about 0.5 wt. %.
Inventors: |
Lu; Yun Martin; (Waukegan,
IL) ; Zhang; Xin; (Waukegan, IL) ; Zheng;
Xiaofeng; (Waukegan, IL) ; Li; Qianqian;
(Waukegan, IL) |
|
Applicant: |
Name |
City |
State |
Country |
Type |
Polymax TPE LLC |
Waukegan |
IL |
US |
|
|
Family ID: |
1000004793799 |
Appl. No.: |
16/855888 |
Filed: |
April 22, 2020 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
|
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62837168 |
Apr 22, 2019 |
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Current U.S.
Class: |
1/1 |
Current CPC
Class: |
C08L 2205/03 20130101;
C08L 23/06 20130101; C08L 2207/04 20130101; C08L 53/00 20130101;
C08L 2207/066 20130101; C08L 91/00 20130101; C08K 5/005
20130101 |
International
Class: |
C08L 23/06 20060101
C08L023/06; C08L 53/00 20060101 C08L053/00; C08L 91/00 20060101
C08L091/00; C08K 5/00 20060101 C08K005/00 |
Claims
1. A thermoplastic elastomer composition, comprising, a polymer
blend comprising from a non-crosslinked elastomer; from about 15
wt. % to about 50 wt. % oil; from about 3.0 wt. % to about 30 wt. %
polyethylene; and from about 0 to about 0.5 wt. % antioxidant.
2. The thermoplastic elastomer composition of claim 1, wherein the
oil comprises mineral oil.
3. The thermoplastic elastomer composition of claim 1, wherein the
non-cross-linked elastomer comprises styrenic block copolymer.
4. The thermoplastic elastomer composition of claim 3, wherein the
styrenic block copolymer is selected from a group consisting of
styrene-butadiene-styrene polymer (SBS), styrene-ethylene
butylene-styrene (SEBS), styrene-isoprene-styrene (SIS),
styrene-isoprene-butadiene-styrene (SIBS), styrene-ethylene
propylene-styrene (SEPS), styrene-ethylene propylene (SEP) block
copolymer, styrene-ethylene ethylene propylene-styrene (SEEPS),
hydrogenated polybutadiene, hydrogenated polyisoprene, hydrogenated
styrene-isoprene random copolymer, poly
(styrene-[(butadiene).sub.1-x-(ethylene-co-butylene)x}-styrene),
wherein x is the hydrogenated fraction of the molecule, and
hydrogenated styrene-butylene random copolymer.
5. The thermoplastic elastomer composition of claim 4, wherein the
styrenic block copolymer comprises
styrene-ethylene-butylene-styrene polymer.
6. The thermoplastic elastomer composition of claim 5, wherein the
styrenic block copolymer comprises about 20 wt. % to about 50 wt. %
styrene-ethylene-butylene-styrene polymer.
7. The thermoplastic elastomer composition of claim 5, wherein the
styrene-ethylene-butylene-styrene polymer total molecular weight is
from about 100,000 to about 440,000 g/mol.
8. The thermoplastic elastomer composition of claim 2, wherein the
mineral oil comprises paraffinic oil.
9. The thermoplastic elastomer composition of claim 7, wherein the
styrene-ethylene-butylene-styrene polymer total molecular weight is
from about 200,000 g/mol to about 440,000 g/mol.
10. The thermoplastic elastomer composition of claim 1, wherein the
polyethylene comprises linear low density polyethylene (LLDPE).
11. The thermoplastic elastomer composition of claim 1, wherein the
styrene-ethylene-butylene-styrene polymer total molecular weight is
from about 240,000 g/mol to about 440,000 g/mol.
12. The thermoplastic elastomer composition of claim 10, wherein
linear low density polyethylene has melt flow index of about 0.5
g/10 min to about 10.0 g/10 min, measured at 230.degree. C.,
employing 2.16 kilogram (kg) weight.
13. The thermoplastic elastomer composition of claim 1, wherein the
thermoplastic elastomer has Shore A hardness from about 20 to
95A.
14. The thermoplastic elastomer composition of claim 1, wherein the
thermoplastic elastomer has a weight percent ratio of
non-crosslinked elastomer to oil, when present, from about 0.4 to
about 2.5.
15. The thermoplastic elastomer composition of claim 14, wherein
the weight percent ratio is from about 0.7 to about 1.5.
16. The thermoplastic elastomer composition of claim 1, wherein the
thermoplastic elastomer has melt viscosity at shear rate of 67 1/s
of about 200 to about 2000 Pas, measured at 200.degree. C.
17. The thermoplastic elastomer composition of claim 1, wherein the
thermoplastic elastomer has melt viscosity at shear rate of 67 1/s
of about 500 to about 1300 Pas, measured at 200.degree. C.
18. The thermoplastic elastomer composition of claim 1, wherein the
thermoplastic elastomer has melt viscosity at shear rate of 67 1/s
of about 200 to about 500 Pas, measured at 200.degree. C.
19. The thermoplastic elastomer composition of claim 1, wherein the
thermoplastic elastomer has melt viscosity at shear rate of 67 1/s
of about 700 to about 1100 Pas, measured at 200.degree. C.
20. The thermoplastic elastomer composition of claim 1, wherein the
non-crosslinked elastomer total molecular weight is from about
100,000 to about 440,000 g/mol.
21. The thermoplastic elastomer composition of claim 1, wherein the
non-crosslinked elastomer total molecular weight is from about
200,000 to about 400,000 g/mol.
22. The thermoplastic elastomer composition of claim 1, wherein the
non-crosslinked elastomer total molecular weight is from about
240,000 to about 400,000 g/mol.
23. A thermoplastic elastomer composition, comprising, a polymer
blend comprising a styrenic block copolymer; from about 15 wt. % to
about 50 wt. % oil; from about 5 wt. % to about 30 wt. %
polyethylene; and from about 0 to about 0.5 wt. % anti-oxidant,
wherein the thermoplastic elastomer has melt viscosity at shear
rate of 67 1/s of about 200 to about 2000 measured at about
200.degree. C.
24. The thermoplastic elastomer composition of claim 23, wherein
the oil comprises mineral oil.
25. The thermoplastic elastomer composition of claim 23, the
styrenic block copolymer is selected from a group consisting of
styrene-butadiene-styrene polymer (SBS), styrene-ethylene
butylene-styrene (SEBS), styrene-isoprene-styrene (SIS),
styrene-isoprene-butadiene-styrene (SIBS), styrene-ethylene
propylene-styrene (SEPS), styrene-ethylene propylene (SEP) block
copolymer, styrene-ethylene ethylene propylene-styrene (SEEPS),
hydrogenated polybutadiene, hydrogenated polyisoprene, hydrogenated
styrene-isoprene random copolymer, poly
(styrene-[(butadiene).sub.1-x-(ethylene-co-butylene)x}-styrene),
wherein x is the hydrogenated fraction of the molecule, and
hydrogenated styrene-butylene random copolymer.
26. The thermoplastic elastomer composition of claim 23, wherein
the styrenic block copolymer comprises
styrene-ethylene-butylene-styrene polymer.
27. The thermoplastic elastomer composition of claim 23, wherein
the styrenic block copolymer comprises about 20 wt. % to about 50
wt. % styrene-ethylene-butylene-styrene polymer.
28. The thermoplastic elastomer composition of claim 27, wherein
the styrene-ethylene-butylene-styrene polymer total molecular
weight is from 100,000 to 440,000 g/mol.
29. The thermoplastic elastomer composition of claim 23, wherein
the mineral oil comprises paraffinic oil.
30. The thermoplastic elastomer composition of claim 28, wherein
the styrene-ethylene-butylene-styrene polymer total molecular
weight is from 2000,000 g/mol to 440,000 g/mol.
31. The thermoplastic elastomer composition of claim 23, wherein
the polyethylene comprises linear low density polyethylene
(LLDPE).
32. The thermoplastic elastomer composition of claim 28, wherein
the styrene-ethylene-butylene-styrene polymer total molecular
weight is from 240,000 g/mol to 440,000 g/mol.
33. The thermoplastic elastomer composition of claim 23, wherein
the thermoplastic elastomer has Shore A hardness from about 20 to
about 95A.
34. The thermoplastic elastomer composition of claim 23, wherein
the thermoplastic elastomer has a weight percent ratio of styrenic
block copolymer to oil, when present, from about 0.4 to about
2.5.
35. The thermoplastic elastomer composition of claim 34, wherein
the weight percent ratio is from about 0.7 to about 1.5.
36. The thermoplastic elastomer composition of claim 23, wherein
the thermoplastic elastomer has melt viscosity at shear rate of 67
1/s of about 200 to about 2000 Pas, measured at 200.degree. C.
37. The thermoplastic elastomer composition of claim 36, wherein
the thermoplastic elastomer has melt viscosity at shear rate of 67
1/s of about 500 to about 1300 Pas, measured at 200.degree. C.
38. The thermoplastic elastomer composition of claim 36, wherein
the thermoplastic elastomer has melt viscosity at shear rate of 67
1/s of about 700 to about 1100 Pas, measured at 200.degree. C.
39. A thermoplastic elastomer composition, comprising, a polymer
blend comprising a styrenic block copolymer, wherein the styrenic
block copolymer is selected from a group consisting of
styrene-butadiene-styrene polymer (SBS), styrene-ethylene
butylene-styrene (SEGS), styrene-isoprene-styrene (SIS),
styrene-isoprene-butadiene-styrene (SIBS), styrene-ethylene
propylene-styrene (SEPS), styrene-ethylene propylene (SEP) block
copolymer, styrene-ethylene ethylene propylene-styrene (SEEPS),
hydrogenated polybutadiene, hydrogenated polyisoprene, hydrogenated
styrene-isoprene random copolymer, poly
(styrene-[(butadiene).sub.1-x-(ethylene-co-butylene)x}-styrene),
wherein x is the hydrogenated fraction of the molecule, and
hydrogenated styrene-butylene random copolymer; from about 15 wt. %
to about 50 wt. % oil; from about 3 wt. % to about 30 wt. %
polyethylene; and from about 0 to about 0.5 wt. % anti-oxidant,
wherein the thermoplastic elastomer has a weight percent ratio of
styrenic block copolymer to oil, when present, from about 0.4 to
about 2.5.
40. The thermoplastic elastomer composition of claim 39, wherein
the oil comprises mineral oil.
41. The thermoplastic elastomer composition of claim 39, wherein
the styrenic block copolymer comprises
styrene-ethylene-butylene-styrene polymer.
42. The thermoplastic elastomer composition of claim 39, wherein
the styrenic block copolymer comprises about 25 wt. % to about 50
wt. % styrene-ethylene-butylene-styrene polymer.
43. The thermoplastic elastomer composition of claim 39, wherein
the mineral oil comprises paraffinic oil.
44. The thermoplastic elastomer composition of claim 39, wherein
the styrene-ethylene-butylene-styrene polymer total molecular
weight is from 200,000 to 440,000 g/mol.
45. The thermoplastic elastomer composition of claim 39, wherein
the polyethylene comprises linear low density polyethylene
(LLDPE).
46. The thermoplastic elastomer composition of claim 39, wherein
the styrene-ethylene-butylene-styrene polymer total molecular
weight is from 240,000 g/mol to 440,000 g/mol.
47. The thermoplastic elastomer composition of claim 39, wherein
the styrene-ethylene-butylene-styrene polymer total molecular
weight is from 100,000 g/mol to 440,000 g/mol.
48. The thermoplastic elastomer composition of claim 39, wherein
the thermoplastic elastomer has Shore A hardness from about 20 to
about 95A.
49. The thermoplastic elastomer composition of claim 39, wherein
the thermoplastic elastomer has a weight percent ratio of styrenic
block copolymer to oil, when present, of from about 0.4 to about
2.5.
50. The thermoplastic elastomer composition of claim 39, wherein
the weight percent ratio is from about 0.7 to about 1.5.
51. The thermoplastic elastomer composition of claim 39, wherein
the thermoplastic elastomer has melt viscosity at shear rate of 67
1/s of about 200 to about 2000 Pas, measured at 200.degree. C.
52. The thermoplastic elastomer composition of claim 39, wherein
the thermoplastic elastomer has melt flow viscosity at shear rate
of 67 1/s of about 500 to about 1300 Pas, measured at 200.degree.
C.
53. The thermoplastic elastomer composition of claim 39, wherein
the thermoplastic elastomer has melt viscosity at shear rate of 67
1/s of about 700 to about 1100 Pas, measured at 200.degree. C.
54. The thermoplastic elastomer composition of claim 39, wherein
the thermoplastic elastomer has viscosity at shear rate of 67 1/s
of about 800 to about 1000 Pas, measured at 200.degree. C.
55. The thermoplastic elastomer composition of claim 39, wherein
the styrenic block copolymer total molecular weight is from 100.000
to 440,000 g/mol.
56. The thermoplastic elastomer composition of claim 39, wherein
the styrenic block copolymer total molecular weight is from 200,000
to 400,000 g/mol.
57. The thermoplastic elastomer composition of claim 39, wherein
the styrenic block copolymer total molecular weight is from 240,000
to 400,000 g/mol.
Description
RELATED PATENT APPLICATIONS
[0001] This application claims priority date of U.S. provisional
application No. 62/837,168, which was filed on Apr. 22, 2019. The
entire disclosures of which are incorporated by reference
herein.
TECHNICAL FIELD
[0002] The present disclosure relates generally to thermoplastic
elastomeric compositions and more specifically to thermoplastic
elastomeric compositions with low compression set and good melt
strength.
BACKGROUND
[0003] A problem that is becoming more evident these days within
the wine industry is that a great number of traditionally naturally
sealed wines are damaged by cork that is tainted, ill-fitting or
deteriorated.
[0004] It is estimated that around 5-10% of all wines have been be
affected to some degree and in some cases the wine will have to be
discarded because the cork is "corked", meaning that the porous and
imperfect material (wood bark) was tainted or infected, and during
its contact with the wine, it altered its chemistry with damaging
results to the quality of the wine. The "corked wine" will be
affected and depending of the seriousness of the taint, it could
show symptoms that go from musty smell, to a change in the tastes
of the wine, which becomes flat and bodiless.
[0005] Therefore, there is a need to develop synthetic wine cork
with elastomeric materials that have low compression set and good
melt strength.
SUMMARY
[0006] According to a first aspect, the thermoplastic elastomer may
comprise a polymer blend. The polymer blend may comprise a
non-crosslinked elastomer, oil, polyethylene, and anti-oxidant. The
oil may be from about 15 wt. % to about 50 wt. %. The polyethylene
may be from about 3.0 wt. % to about 30 wt. %. The anti-oxidant may
be from about 0 to about 0.5 wt. %.
[0007] In certain aspects, the oil comprises mineral oil.
[0008] In certain aspects, the non-crosslinked elastomer may
comprise styrenic block copolymer.
[0009] In certain aspects, the styrenic block copolymer may be
selected from a group consisting of
styrene-ethylene-butadiene-styrene polymer, styrene-ethylene
butylene-styrene, styrene-ethylene propylene-styrene (SEPS),
hydrogenated polybutadiene, hydrogenated polyisoprene, hydrogenated
styrene-isoprene random copolymer, styrene-ethylene propylene (SEP)
block copolymer, styrene-ethylene ethylene propylene-styrene
(SEEPS), and hydrogenated styrene-butadiene random copolymer.
[0010] In certain aspects, the styrenic block copolymer may
comprise styrene-ethylene-butylene-styrene polymer.
[0011] In certain aspects, the styrenic block copolymer may
comprise about 20 wt. % to about 50 wt. %
styrene-ethylene-butylene-styrene polymer.
[0012] In certain aspects, the styrene-ethylene-butylene-styrene
polymer total molecular weight is from 100,000 to 440,000
g/mol.
[0013] In certain aspects, the mineral oil may comprise paraffinic
oil.
[0014] In certain aspects, the styrene-ethylene-butylene-styrene
polymer total molecular weight is from 200,000 g/mol to 440,000
g/mol. In certain aspects, the polyethylene may comprise linear low
density polyethylene (LLDPE).
[0015] In certain aspects, the styrene-ethylene-butylene-styrene
polymer total molecular weight is from 240,000 g/mol to 440,000
g/mol. In certain aspects, linear low density polyethylene has melt
flow index of about 0.5 to about 10.0 g/10 min, measured at
230.degree. C., employing 2.16 kilogram (kg) weight.
[0016] In certain aspects, the thermoplastic elastomer has Shore A
hardness from about 30 to 95A.
[0017] In certain aspects, the thermoplastic elastomer has a weight
percent ratio of non-crosslinked elastomer to oil, when present,
from about 0.4 to about 2.5.
[0018] In certain aspects, the weight percent ratio is from about
0.7 to about 1.5.
[0019] In certain aspects, the thermoplastic elastomer has melt
viscosity at shear rate of 67 1/s of about 200 to about 2000 Pas,
measured at 200.degree. C.
[0020] In certain aspects, the thermoplastic elastomer has melt
viscosity at shear rate of 67 1/s of about 500 to about 1300 Pas,
measured at 200.degree. C.
[0021] In certain aspects, the thermoplastic elastomer has melt
viscosity at shear rate of 67 1/s of about 200 to about 500 Pas,
measured at 200.degree. C.
[0022] In certain aspects, the thermoplastic elastomer has melt
viscosity at shear rate of 67 1/s of about 700 to about 1100 Pas,
measured at 200.degree. C.
[0023] In certain aspects, the non-crosslinked elastomer total
molecular weight is from about 100,000 to about 440,000 g/mol.
[0024] In certain aspects, the non-crosslinked elastomer total
molecular weight is from about 200,000 to about 400,000 g/mol.
[0025] According to a second aspect, a thermoplastic elastomer may
comprise a polymer blend. The polymer blend may comprise a styrenic
block copolymer, oil, polyethylene, anti-oxidant. The oil may be
from about 15 wt. % to about 50 wt, %. The polyethylene may be from
about 3 wt. % to about 30 wt, %. The anti-oxidant may be from about
0 to about 0.5 wt. % anti-oxidant. The thermoplastic elastomer may
have melt viscosity at shear rate of 67 1/s of about 200 to about
2000 measured at about 200.degree. C. According to a second aspect,
a thermoplastic elastomer may comprise a polymer blend. The polymer
blend may comprise a styrenic block copolymer, oil, polyethylene,
and anti-oxidant. The oil may be from about 15 wt. % to about 50
wt. %. The polyethylene may be from about 3 wt. % to about 30 wt.
%. The anti-oxidant may be from about 0 to about 0.5 wt. %
anti-oxidant. The thermoplastic elastomer may have a weight percent
ratio of styrenic block copolymer to oil, when present, from about
0.4 to about 2.5. The styrenic block copolymer may be selected from
a group consisting of styrene-ethylene-butylene-styrene polymer,
styrene-ethylene butylene-styrene, styrene-ethylene
propylene-styrene (SEPS), styrene-ethylene propylene (SEP) block
copolymer, styrene-ethylene ethylene propylene-styrene (SEEPS), and
hydrogenated styrene-butadiene random copolymer.
DETAILED DESCRIPTION
[0026] In the following description, well-known functions or
constructions are not described in detail because they may obscure
the disclosure in unnecessary detail. For this disclosure, the
following terms and definitions shall apply. 1271 Reference
throughout this specification to "one embodiment" or "an
embodiment" means that a particular feature, structure, or
characteristic described in connection with the embodiment is
included in at least one embodiment of claimed subject matter.
Thus, the appearances of the phrase "in one embodiment" or "an
embodiment" in various places throughout this specification are not
necessarily all referring to the same embodiment. Furthermore, the
particular features, structures, or characteristics may be combined
in one or more embodiments.
[0027] Additionally, variations to the disclosed embodiments can be
understood and effected by the skilled person in practicing the
claimed disclosure, the disclosure, and the appended claims. In the
claims, the word "comprising" does not exclude other elements or
steps, and the indefinite article "a" or "an" does not exclude a
plurality. The mere fact that certain measures are recited in
mutually different dependent claims does not indicate that a
combination of these measures cannot be used to advantage.
[0028] Also, two or more steps may be performed concurrently or
with partial concurrence. Further, the steps of the method may be
performed in an order different from what has been disclosed. Such
variation will depend on the process hardware systems chosen and on
designer choice. All such variations are within the scope of the
disclosure. Additionally, even though the disclosure has been
described with reference to specific exemplifying embodiments
thereof, many different alterations, modifications and the like
will become apparent for those skilled in the art.
[0029] Embodiments include thermoplastic elastomeric material
compositions, processes for preparing the compositions and articles
of manufacture prepared from the compositions. In one embodiment,
the thermoplastic elastomeric composition is provided comprising a
polymer blend of about 15% to about 50%
styrene-ethylene-butadiene-styrene (SEGS) polymer; from about 15%
to about 50% oil; from about 3.0% to about 30% polyethylene; and
from about 0 to about 0.5% anti-oxidant.
[0030] As used herein, the term "polymer" refers to the product of
a polymerization reaction, and is inclusive of homopolymers,
copolymers, terpolymers, etc.
[0031] As used herein, unless specified otherwise, the term
"copolymer(s)" refers to polymers formed by the polymerization of
at least two different monomers. For example, the term "copolymer"
includes the copolymerization reaction product of ethylene and an
alpha-olefin, such as 1-hexene. However, the term "copolymer" is
also inclusive of, for example, the copolymerization of a mixture
of ethylene, propylene, 1-hexene, and 1-octene.
[0032] As used herein, when a polymer is referred to as "comprising
a monomer," the monomer is present in the polymer in the
polymerized form of the monomer or in the derivative form the
monomer.
[0033] As used herein, "molecular weight" means weight average
molecular weight ("Mw"). Mw is determined using Gel Permeation
Chromatography. Molecular Weight Distribution ("MWD") may be
defined or measured as Mw divided by number average molecular
weight ("Mn"). (For more information, see U.S. Pat. No. 4,540,753
to Cozewith et al. and references cited therein, and in Ver Strate
et al., 21 MACROMOLECULES, pp. 3360-3371 (1998)). The "Mz" value is
the high average molecular weight value, calculated as discussed by
A. R. Cooper in Concise Encyclopedia of Polymer Science and
Engineering, pp. 638-639 (J. I. Kroschwitz, ed. John Wiley &
Sons 1990).
[0034] The term "active agent" refers to a substance capable of
delivering special activity or function to users. Suitable active
agents may be in a variety of geometric forms including discrete
particles, fibers, flakes, rods, spheres, needles, particles coated
with fibers and the like.
[0035] The term "compression" refers to the process or result of
pressing by applying a force on an object, thereby increasing the
density of the object.
[0036] The terms "elastomeric," "elastomer," "elastic," and other
derivatives of "elastomeric" are used interchangeably and refer to
materials having elastomeric or rubbery properties. Elastomeric
materials, such as thermoplastic elastomers and thermoplastic
vulcanizates, are generally capable of recovering their shape after
deformation when the deforming force is removed. Specifically, as
used herein, elastomeric is meant to be that property of any
material which upon application of an elongating force, permits
that material to be stretchable to a stretched length which is at
least about 25 percent greater than its relaxed length, and that
will cause the material to recover at least 40 percent of its
elongation upon release of the stretching elongating force. A
hypothetical example which would satisfy this definition of an
elastomeric material in the X-Y planar dimensions would be a one
(1) inch sample of a material which is elongatable to at least 1.25
inches and which, upon being elongated to 1.25 inches and released,
will recover to a length of not more than 1.15 inches. Many
elastomeric materials may be stretched by much more than 25 percent
of their relaxed length, and can recover to substantially their
original relaxed length upon release of the stretching, elongating
force. In addition to a material being elastomeric in the described
X-Y planar dimensions of a structure, including a web or sheet, the
material can be elastomeric in the Z planar dimension.
Specifically, when a structure is compressively loaded, it displays
elastomeric properties and will essentially recover to its original
position upon removal of the load. Compression set is sometimes
used to help describe such elastic recovery. When compression is
applied to an elastomeric structure, the structure may display
elastomeric properties and then recover to near its original
position upon relaxation.
[0037] The term "extensible" refers to a material that is generally
capable of being extended or otherwise deformed, but which does not
recover a significant portion of its shape after the extension or
deforming force is removed.
[0038] The term "flexible" refers to the ability of a material to
bend under an imposed load such that its Bending Modulus at 0.5 mm
deflection is 1000 g/mm or lower as measured by the Bending Modulus
Test.
[0039] The term "thermoplastic" describes a material that softens
and/or flows when exposed to heat and which substantially returns
to its original hardened condition when cooled to room
temperature.
[0040] As used herein, "weight percent" or "wt. %", unless noted
otherwise, means a percent by weight of a particular component
based on the total weight of the composition containing the
component. For example, if a mixture contains three pounds of sand
and one pound of sugar, then the sand comprises 75 wt. % (3 lbs.
sand/4 lbs. total mixture) of the mixture and the sugar 25 wt.
%.
[0041] The term "crystalline" if employed, refers to a polymer or a
segment that possesses a first order transition or crystalline
melting point (Tm) as determined by differential scanning
calorimetry (DSC) or equivalent technique. The term may be used
interchangeably with the term "semicrystalline". The term
"amorphous" refers to a polymer lacking a crystalline melting point
as determined by differential scanning calorimetry (DSC) or
equivalent technique.
[0042] As used herein, Melt Flow Rates ("MFR") may be determined in
accordance with ASTM D1238 at 230.degree. C. and 2.16 kg
weight.
[0043] As used herein, Melt Indices ("MI") or Melt Flow
Index/Indices, also may be known as Melt Flow Rates, which may be
determined in accordance with ASTM D1238 at 190.degree. C. and 2.16
kg weight.
[0044] Unless otherwise indicated, all numbers expressing
quantities of ingredients, properties such as molecular weight,
reaction conditions, properties such as molecular weight, reaction
conditions, and so forth used in the specification and claims are
to be understood as being modified in all instances by the term
"about." Accordingly, unless indicated to the contrary, the
numerical parameters set forth in the following specification and
attached claims are approximations that may vary depending upon the
desired properties sought to be obtained by the present invention.
At the very least, and not as an attempt to limit the application
of the doctrine of equivalents to the scope of the claims, each
numerical parameter should at least be construed in light of
reported significant digits and by applying ordinary rounding
techniques.
[0045] Notwithstanding that the numerical ranges and parameters set
forth the broad scope of the invention are approximations, the
numerical values set forth in specific examples are reported as
precisely as possible. Any numerical value, however, inherently
contain certain errors necessarily resulting from the standard
deviation found in their respective testing measures.
[0046] The thermoplastic elastomeric compositions may comprise a
polymer blend. The polymer blend may comprise a non-crosslinked
elastomer, oil, polyethylene, and an antioxidant.
[0047] Preferred styrenic block copolymers are those having the
formulae: ABA, (A-B) nX, ABAB' or ABA'B' respectively, wherein A
and A' represent a poly (monovinyl aromatic) block and B and B'
represent hydrogenated poly (conjugated diene(s)) blocks, wherein n
is an integer .gtoreq.2 and wherein X is the remainder of a
coupling agent. It will be appreciated that the blocks A and A',
and B and B' respectively are equal or different from each other,
in that the blocks A are larger than the blocks A' and the blocks B
are larger than B' or B and B' are equal.
[0048] Most preferred block copolymers have the formulae ABA or
(A-B)nX, wherein A represents a polymer block of one or more
monovinyl aromatic monomers selected from styrene, C1-C4 alkyl
styrene and C1-C4dialkylstyrene and in particular styrene,
.alpha.-methyl styrene, o-methyl styrene or p-methyl styrene,
1,3-dimethylstyrene, p-tert-butyl styrene or mixtures thereof and
most preferably styrene only, wherein B represents a polymer block
of one or more conjugated diene monomers containing from 4 to 8
carbon atoms, such as 1,3-butadiene, 2-methyl-1,3-butadiene
(isoprene), 2,3-dimethyl-1,3-butadiene or mixtures thereof, and
preferably butadiene or isoprene and most preferably butadiene.
[0049] Preferred block copolymers ABA or (A-B)nX comprise
substantially pure poly(styrene) blocks, each having a true
molecular weight in the range of from 3 kg/mole to 50 kg/mole while
the total apparent molecular weight is in the range of from 70 to
700 kg/mol and preferably from 100 to 500 kg/mol. The molecular
weights referred to in this specification and claims can be
measured with gel permeation chromatography (GPC) using polystyrene
calibration standards, such as is done according to ASTM 3536. GPC
is a well-known method wherein polymers are separated according to
molecular size, the largest molecule eluting first. The
chromatograph is calibrated using commercially available
polystyrene molecular weight standards. The molecular weight of
polymers measured using GPC so calibrated are apparent molecular
weights, also known as styrene equivalent molecular weights. The
styrenic equivalent molecular weight may be converted to true
molecular weight when the styrenic content of the polymer and the
vinyl content of the diene segments are known. The detector used is
preferably a combination ultraviolet and refractive index detector.
The molecular weights expressed herein are measured at the peak of
the GPC trace, converted to true molecular weights, and are
commonly referred to as "peak molecular weights".
[0050] Preparation methods for such polymers may be found in U.S.
Pat. Nos. 3,231,635, 3,231,635, 3,231,635, 3,231,635, and
3,231,635, in U.S. Pat. No. 3,231,635. U.S. Pat. No. 3,231,635.
U.S. Pat. No. 3,231,635. and in U.S. Pat. No. 3,231,635. Processes
for the selective hydrogenation of the B blocks were known from
e.g. U.S. Pat. No. 3,231,635. U.S. Pat. No. 3,231,635. U.S. Pat.
No. 3,231,635. U.S. Pat. Nos. 3,231,635, and 3,231,635. The
disclosures of these before mentioned documents are herein
incorporated by reference.
[0051] Suitable representatives of said most preferred block
copolymers are those available under the trade names KRATON.RTM.,
SEPTON.TM. and TUFTEC.TM., for instance KRATON G 1650, KRATON G
1654. KRATON G 1651, KRATON G 1652, KRATON G 1633, KRATON G 1641,
KRATON G 1657, KRATON A 1535, KRATON A 1636, KRATON GRP 6924,
SEPTON 4055, SEPTON 4077, TUFTEC H 1272, TSRC Taipol 6150, Taipol
6154, Taipol 6151, Taipol 6159, Sinopec 503T, 602T and 604T
comprising usually poly(conjugated diene) blocks being hydrogenated
until less than 10% of the original ethylenic unsaturation.
[0052] The block copolymers that may be used in this embodiment may
be selected from the group of styrene-ethylene butylene-styrene
(SEBS), styrene-ethylene propylene-styrene (SEPS), hydrogenated
polybutadiene, hydrogenated polyisoprene, hydrogenated
styrene-isoprene random copolymer, styrene-ethylene propylene (SEP)
block copolymer, styrene-ethylene ethylene propylene-styrene
(SEEPS) and hydrogenated styrene-butadiene random copolymer.
[0053] The hydrogenation of random diene copolymers are described
by authors E. W. Duck, J. R. Hawkins, and J. M. Locke, in Journal
of the IRI, 6, 19, 1972, which may be used as the highly saturated
elastomer in this invention and is incorporated herein as a
reference. The saturated triblock polymers, SEBS and SEPS, with
styrenic end blocks are also used in this invention as the
saturated elastomers. SEBS and SEPS are obtained on the
hydrogenation of triblock copolymers of styrenic and butadiene or
styrenic and isoprene and are known to be commercially available.
Some commercially available examples of such elastomers include
Kraton G series polymers. U. S. Pat. Nos. 3,686,364 and 3,865,776
give some examples of block copolymers that may be used in the
practice of this invention and are incorporated herein by
reference. It is highly preferred that the highly saturated
elastomer be SEBS having a bound styrenic content that is within
the range of 15 weight percent to about 60 weight percent.
[0054] It is possible to use the saturated block copolymers that
are modified versions of SEBS. Such modified block copolymers
additionally have a substantial number of styrenic units that are
randomly distributed in the rubber mid blocks of ethylene and
butylene. These modified saturated block copolymers are supplied
under Kraton `A` series. Saturated block copolymers grades as
mentioned in TPE 2003 RAPRA Conference Proceedings, Brussels,
Belgium, Sep. 16-17, 2003, Paper 18, Page 157, and Paper 21, page
181 may also be used and are incorporated herein by reference.
[0055] In one embodiment, polystyrene-ethylene-butadiene-styrene
(SEBS) block copolymer may include suitable SEBS copolymers that
include those with a block styrenic content of about 10 to about 35
wt. % based on the total SEBS copolymer, and have Shore A hardness
values of about 40 to about 80.
[0056] The thermoplastic elastomeric may comprise about 0.1 wt. %
to about 40 wt. % polyethylene, more preferably about 1.0 wt. % to
about 35 wt. % polyethylene, more preferably 3.0 wt. % to about 30
wt. % polyethylene, more preferably, 4.0 wt. % to about 25 wt. %
polyethylene. Suitable polyethylene may include high density
polyethylene (HDPE), low density polyethylene (LDPE), and linear
low density polyethylene (LLDPE). In one embodiment, high molecular
weight polyethylene compounds may be used. In one embodiment,
suitable linear low density polyethylene (LLDP) generally have melt
indices of about 0.5 to about 10.0 g/10 min, measured at
230.degree. C., employing 2.16 kilogram (kg) weight.
[0057] The thermoplastic elastomeric compositions may comprise up
to about 60% wt. %, preferably about 15 wt. % to about 55 wt. %
oil, more preferably about 15 wt. % to about 50 wt. % oil, for
example. Suitable oil may include mineral oil. Suitable mineral oil
may include paraffinic oils (ASTM D2226 TYPE 104), or naphthenic
oils (ASTM 103 & 104A). All above oils represent different cuts
from the distillation of crude oil.
[0058] In addition, the thermoplastic elastomeric compositions may
comprise up to about 2 wt. %, preferably up to about 1 wt. %
anti-oxidant, more preferably up to about 0.5% wt. % antioxidant.
Suitable anti-oxidant may include hindered phenols, thiol
compounds, amines or phosphites.
[0059] The thermoplastic elastomeric compositions also may comprise
up to about 3 wt. % colorant. Suitable color pigments are known to
those skilled in the art and the exact amount of color pigment is
readily empirically determined based on the desired color
characteristic of the composition and the finished product.
[0060] The thermoplastic elastomeric compositions may also comprise
up to about 3 wt. %, preferably about 1 wt. %, of a processing aid
such a metal stearate, soaps, an ultra-high molecular weight
siloxane polymer or lubricants, in order to assist proper flow of
the polymer melt through the injection molded barrel and dies and
result in molded parts with good surface characteristics. A
suitable example is zinc stearate.
[0061] The thermoplastic elastomeric compositions may also
optionally comprise stabilizers, such as heat stabilizer and/or
light stabilizer, such as ultraviolet light stabilizers, as well as
combinations of heat and light stabilizers. Heat stabilizers, like
antioxidants, include phenolics, amines, phosphites, and the like,
as well as combinations comprising at least one of the foregoing
heat stabilizers. Light stabilizers include low molecular weight
(having number-average molecular weights less than about 1,000 AMU)
benzophenones or hindered amines, high molecular weight (having
number-average molecular weights greater than about 1,000 AMU)
hindered amines, benzotriazoles, hydroxyphenyl triazines, and the
like, as well as combinations comprising at least one of the
foregoing light stabilizers. Optionally, various additives known in
the art may be used as needed to impart various properties to the
composition, such as heat stability, stability upon exposure to
ultraviolet wavelength radiation, long-term durability, and
processability. The exact amount of stabilizer is readily
empirically determined by the reaction employed and the desired
characteristics of the finished article, with up to about 3 wt. %
possible, 1 wt. % preferred.
[0062] The thermoplastic elastomeric compositions and articles
formed thereof may be prepared in a process. In the present
process, the polymer blend comprised of a thermoplastic elastomer
material, such as styrene-ethylene-butadiene-styrene (SEBS) polymer
in powder form, is pre-mixed with polyethylene, anti-oxidant, and
oil using a high shear mixer or other such device to form a tumble
mixed blend of the composition prior to being disposed into the
hopper of the twin screw extruder, through which the premix is
melted, mixed and pelletized in to thermoplastic elastomer pellets.
The formed Thermoplastic elastomer can be processed into different
products such as wine corks, toothpicks and others by extrusion
process, injection molding and other polymer processing
processes.
EXPERIMENTAL DETAILS
[0063] Mixing in a continuous process typically occurs in a
twin-screw extruder that was elevated to a temperature that was
sufficient to melt the polymer matrix with addition of all
additives at the feed-throat, or by injection or side-feeders
downstream. Extruder speeds ranged from about 50 to about 1200
revolutions per minute (rpm), and preferably from about 300 to
about 700 rpm, for example. Typically, the output from the extruder
was pelletized for later processing. By the use of a twin-screw
extruder, the blending components as shown hereunder were kneaded
at from about 160.degree. C. to about 220.degree. C., and extruded
into strands, which were then cut into pellets. For example, a lab
twin screw extruder included 9 zones, with zone 1 about 160.degree.
C., zone 2 about 180.degree. C., zone 3 about 210.degree. C., zone
4 about 210.degree. C., zone 5 about 200.degree. C., zone 6 about
180.degree. C., zone 7 about 160.degree. C., zone 8 about
160.degree. C., zone 9 about 160.degree. C. The pelletizer
temperature may be 170.degree. C.
Examples 1-4
[0064] A composition of pellet form was prepared in accordance with
the compounding recipe shown in Table 1, using a twin-screw
extruder under conditions discussed in experiment details. The
pellets were injection-molded to prepare a square sheet of 10
cm.times.10 cm. The sheet was cut by a dumbbell cutter to prepare
test pieces for measurement. In the preparation of the composition
in the twin-screw extruder, Components were dry-blended; the blend
was passed through the extruder. The results are shown in Table
2.
[0065] As is clear from Table 2, the Elastomer Compositions of this
embodiment are elastomers having a low compression set, excellent
elasticity and excellent dynamic properties.
TABLE-US-00001 TABLE 1 14A 14B 14C 1A Raw Material Name pphr % pphr
% pphr % phbr % SEBS 1633 100.00 31.50 100.00 31.50 100.00 30.35
100.00 32.00 Drakeol 600 121.00 38.12 121.00 38.21 121.00 36.73
121.00 38.72 Polypropylene 23.00 7.25 0.00 0.00 0.00 0.00 0.00 0.00
6523 Polypropylene 0.00 0.00 23.00 7.25 0.00 0.00 0.00 0.00 Inspire
114 Polyastolyn 10.00 3.15 10.00 3.15 10.00 3.04 10.00 3.20 290
LLDPE 23.00 7.25 23.00 7.25 58.00 17.61 0.00 0.00 SP4030 Armoslip E
0.25 0.08 0.25 0.08 0.25 0.08 0.25 0.08 Irogonox 0.20 0.06 0.20
0.06 0.20 0.06 0.21 0.07 1010 Vicron 25-11 40.00 12.00 40.00 12.60
40.00 12.14 40.00 12.80 Polypropylene 0.00 0.00 0.00 0.00 0.00 0.00
41.00 13.12 CP360H TOTAL 317.45 100.00 317.45 100.00 329.45 100.00
312.46 100.00 Density 0.990 1.008 0.997 0.982 (gram/cm.sup.2)
TABLE-US-00002 TABLE 2 Group 14A, 14B, 14C, 1A test result summary
14A 14B 14C 1A Hardness, Shore A 61 62 64 60 Density, g/cm.sup.3
0.98 0.99 0.99 0.98 Compression Set, 34.41% 36.34% 29.15% 41.01%
70.degree. C.@22 hrs Tensile Strength, MPa 5.70 5.31 6.01 8.19
Tensile Elongation, % 436 288 142 571 100% Modulus, MPa 2.89 3.63
4.87 2.66 300% Modulus, MPa 4.46 / / 4.24 Viscosity(200.degree.
1095.24 1168.71 1464.54 653.70 C.)@Shear Rats 67 1/S, Pa*s
Examples 5-9
[0066] A composition of pellet form was prepared in accordance with
the compounding recipe shown in Table 3, using a twin screw
extruder under conditions discussed in experiment details. The
pellets were injection-molded to prepare a square sheet of 10
cm.times.10 cm. The sheet was cut by a dumbbell cutter to prepare
test pieces for measurement. In the preparation of the composition
in the twin screw extruder, Components were dry-blended; the blend
was passed through the extruder. The results are shown in Table
4.
[0067] As is clear from Table 4, the Elastomer Compositions of this
embodiment are elastomers having a low compression sets, excellent
elasticity and good melt strength.
TABLE-US-00003 TABLE 3 A B C D E Raw material Name pphr % pphr %
pphr % phbr % phbr % SEBS 100.00 35.57 100.00 35.57 100.00 35.57
100.00 35.57 100.00 35.57 503T Drakeol 121.00 43.04 121.00 43.04
121.00 43.04 121.00 4304 121.00 43.04 34 LLDPE 30.00 10.67 15.00
5.34 0.00 0.00 45.00 16.01 60.00 21.34 SP4030 PP6523 30.00 10.67
45.00 16.01 60.00 21.34 15.00 5.34 0.00 0.00 BNX1010 0.14 0.05 0.14
0.05 0.14 0.15 0.14 0.05 0.14 0.05 TOTAL 281.14 100.00 281.14
100.00 281.14 100.00 281.14 100.00 281.14 100.00
TABLE-US-00004 TABLE 4 A B C D E Hardness, Shore A 69 73 77 63 61
Density, g/cm.sup.3 0.88 0.88 0.88 0.91 0.91 Compression Set, 45.1%
.sup. 48% 54.7% 38.4% .sup. 34% 70.degree. C.@22 hours Compression
Set, 18.2% 18.8% 22.1% .sup. 15% 12.7% 23.degree. C.@22 hours
Tensile Tensile Strength, MPa 5.60 5.65 7.10 6.36 6.38 Tensile
Elongation, % 374 228 349 498 477 50% Modulus, MPa 3.10 3.95 4.59
2.09 1.50 100% Modulus, MPa 3.81 4.70 5.28 2.68 2.16 200% Modulus,
MPa 4.60 5.42 5.99 3.56 3.30 300% Modulus, MPa 5.19 5.93 6.51 4.39
4.36 Rheology Viscosity(200.degree. C.)@Shear 810.32 695.22 575.73
916.81 1064.23 Rate 67 1/S, Pa*s
Examples 10-15
[0068] A composition of pellet form was prepared in accordance with
the compounding recipe shown in Table 5, using a twin screw
extruder under conditions discussed in experiment details. The
pellets were injection-molded to prepare a square sheet of 10
cm.times.10 cm. The sheet was cut by a dumbbell cutter to prepare
test pieces for measurement. In the preparation of the composition
in the twin screw extruder, Components were dry-blended; the blend
was passed through the extruder. The results are shown in Table
6.
[0069] As is clear from Table 6, the Elastomer Compositions of this
embodiment are elastomers having a low hardness, compression sets,
excellent elasticity, and good melt strength.
TABLE-US-00005 TABLE 5 177A 177B 177C 177D 178A 178B Raw Material
Name pphr % pphr % pphr % phbr % phbr % ppbr % SEBS 0.00 0.00 0.00
0.00 0.00 0.00 100.00 40.01 1633 SEBS 100.00 43.49 100.00 40.01
100.00 42.56 0.00 0.00 100.00 39.69 100.00 37.32 1651 Drakeol
110.00 47.84 110.00 44.01 100.00 42.56 110.00 44.01 110.00 43.66
116.00 43.29 600 Polypropylene 8.00 3.48 18.00 720 16.00 6.81 18.00
7.20 Inspire 114 PP 6523 19.00 7.54 24.00 8.96 Alathon .RTM. 8.00
3.48 18.00 7.20 16.00 6.81 18.00 7.20 19.00 7.54 0.00 0.00 HDPE
H5618 Irgonox 0.15 0.07 0.15 0.06 0.15 0.06 0.15 0.06 1010 BNX 0.15
0.06 0.15 0.06 1010 Armoslip 0.50 0.22 0.50 0.20 0.50 0.21 0.50
0.20 0.50 0.20 0.20 0.19 E BNX 0.30 0.13 0.30 0.12 0.30 1.28 3.00
1.20 0.30 0.12 0.30 0.11 DLTDP MB50002 3.00 1.30 3.00 1.20 3.00
1.28 3.00 1.20 3.00 1.19 3.00 Silicone MASTER BATCH
TABLE-US-00006 TABLE 6 Hardness, Compression testing No. Shore A
Set condition Protocol 177A 41 41.8 70.degree. C., 22 h ASTM D359B
177B 58 38 70.degree. C., 22 h ASTM D359B 177C 58 40.1 70.degree.
C., 22 h ASTM D359B 177D 59 35.7 70.degree. C., 22 h ASTM D359B
178A 58 46.2 70.degree. C., 22 h ASTM D359B 178B 60 45 70.degree.
C., 22 h ASTM D359B
[0070] The embodiments of the present compositions, processes and
articles made there from, although primarily described in relation
to wine cork skin application, may be utilized in numerous other
applications, both nonautomotive and automotive vehicle
applications such as interior sheathing, including instrument panel
skins, door panels, air bag covers, roof liners, and seat
covers.
[0071] It will be understood that a person skilled in the art may
make modifications to the embodiments shown herein within the scope
and intent of the claims. While the present invention has been
described as carried out in specific embodiments thereof, it is not
intended to be limited thereby but is intended to cover the
invention broadly within the scope of the claims.
[0072] The above-cited patents and patent publications are hereby
incorporated by reference in their entirety. Although various
embodiments have been described with reference to a particular
arrangement of parts, features, and like, these are not intended to
exhaust all possible arrangements or features, and indeed many
other embodiments, modifications, and variations may be
ascertainable to those of skill in the art, Thus, it is to be
understood that the invention may therefore be practiced otherwise
than as specifically described above.
* * * * *